- Staat
- TX
- Alter
- 1,2
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Infection
Rash morbilliform
Symptomtext
Measles like rash within 14 days of infection, no fever, well appearing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash morbilliform
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 1,1
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash macular
Rash papular
Symptomtext
Rash began on her torso and face. Very small pink dots. Was not raised. The next morning the rash was much worse, Covering all of her face, into her scalp. Rash spread to her arms and legs on day #2 and 3. Slightly raised. She was not bothered by rash, did not have a fever. She still currently has small pink dots that are not as bright pink as on day #2 and Day #3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Balance disorder
Dizziness
Headache
Pain
Symptomtext
Body aches, headache, light headedness, imbalance and left sided joint pain. Appointment with Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypertension and Hypothyroidism
- Andere Medikamente
- Potassium, Octi Health Supplement, B12 and Folic Acid, Promethazine, levothyroxine, HCTZ and Vitamins D and E
- Allergien
- Cilantro, Codeine and Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Symptomtext
Left Upper Arm pain and swelling around site of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Band neutrophil percentage
Blood culture negative
Blood fibrinogen normal
C-reactive protein increased
Culture urine negative
Enterovirus test positive
Eosinophil percentage decreased
Erythema multiforme
Full blood count
Human rhinovirus test positive
Lymphocyte percentage increased
Neutrophil percentage decreased
Procalcitonin
Pyrexia
Rash
Rash erythematous
Rash macular
Red blood cell sedimentation rate normal
Symptomtext
Patient vaccinated 5/10. At same time diagnosed with acute otitis media and prescribed amoxicillin twice daily. No missed doses. Starting 5/18 PM was noted to have erythematous patchy rash on trunk and lower extremities. 5/19 started with fever (102F rectal), rash spread to include larger erythematous patches with dusky centers. Patient was advised to stop amoxicillin after taking AM dose on 5/19, transitioned to azithromycin. 5/20 progression of rash to targetoid lesions. presented to ED on 5/21 with diffuse erythematous rash on trunk with some scattered macular areas on neck and extremities. Pt evaluated by pediatric infectious diseases and diagnosed with erythema multiforme, suspect related to amoxicillin. Patient treated with supportive care with full resolution of symptoms and discharge on 5/23/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 2,0
- Labordaten
- 5/21: CBC 9.9>10<309, 24% neutrophils, 30% bands, 46% lymphocytes, no eosinophils; ESR 10mm/hr; CRP 87mg/L; procalcitonin 0.9; fibrinogen wnl; HS trophonin wnl: COVID 19: IgG: reactive (quant: 3.43); RVP: rhino/enterovirus positive; UA: normal; blood and urine cultures remain negative.
- Aktuelle Erkrankungen
- Acute otitis media diagnosed at well child visit were he received his 12mo vaccines.
- Vorgeschichte
- none
- Andere Medikamente
- Prescribed 5/10/22 (same day as vaccination) amoxicillin, dose unknown, for acute otitis media. Completed 8 days. Discontinued on 5/18/22 due to new onset rash (later diagnosed as erythema multiforme) with concern for adverse drug reaction
- Allergien
- none prior to event
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Irritability
Pyrexia
Rash
Rash erythematous
Rash pruritic
Rash vesicular
Teething
Urticaria
Viral rash
Symptomtext
Patient given 12 months vaccines on 4/25/22 (MMR II, Varivax, Prevnar 13). 2 days later on 4/27/22 mother reports that child started with rash to abdomen, chest, and back, that also present to arms and legs at times. The rash was red flat areas with some whelps. Itchy rash to child. The rash would come and go and still present. Presented today for an appointment. Looks similar to vaccine Varicella like rash versus viral rash. X2 insect bites with some redness to right posterior leg. Fevers, irritability, and poor appetite for 3-4 days after vaccines. Still some clinging and decreased appetite. Child also teething. Denies SOB or difficulty breathing, denies swelling lips/tongue. Rash is worse with hot bath or playing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Rash
Symptomtext
Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Additional Details: she developed rash on the left side of her body about 2 weeks after the vaccine. mmr vaccine was given sc in left arm. started with small rash and got larger. got rx from dr today 4/25/22 for triamcinolone crm and an antifungal crm. is going on beach vacation soon and wants rash resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 20.06.2023
- Impfdatum
- 19.06.2023
- Beginn
- 19.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given an MMR vaccine that was expired by 1 day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None, patient has not had an adverse reaction.
- Aktuelle Erkrankungen
- asthma
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.09.2022
- Impfdatum
- -
- Beginn
- 31.08.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
Confirmed with caller no other AE occurred; Customer reported an AE for VARIVAX and MMRII. The caller said these products were administered to the patient after two temperature excursions occurred; This spontaneous report has been received from a consumer concerning a patient of unknown age and gender. The patient's medical history, drug reactions or allergies, concurrent conditions and concomitant medications were not reported. On an unknown date, two temperature excursions occurred for varicella virus vaccine live (oka/merck) (VARIVAX) and measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) with a temperature of 5.9 and 8.8 degrees Celsius, for a time frame of 10 and 8 hours. No previous temperature excursions were reported. On 31-AUG-2022, the patient was administered varicella virus vaccine live (oka/merck) (VARIVAX) 1 dose, lot # U028164, expiration date 09-SEP-2023; and measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (recombinant human albumin [rHA]) (M-M-R II) 1 dose, lot # U019291 expiration date 18-JUN-2023 (route of administration and anatomical location were not provided) both as prophylaxis (product storage error). No other events were reported (no adverse event).; Sender's Comments: US-009507513-2209USA003954: US-009507513-2209USA004005:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No other adverse events occurred; The caller said these products were administered to the patient after two temperature excursions occurred.; This spontaneous report was received from a consumer concerning a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 02-SEP-2022, the patient was vaccinated with 1 dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (rHA) (M-M-R II) subcutaneous injection, lot #U019291, expiration date: 18-JUN-2023 (strength, and route of administration were not provided); and 1 dose of varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection, lot #U028164, expiration date: 09-SEP-2023 (strength, and route of administration were not provided), both administered as prophylaxis. The reporter stated that the vaccines experienced two temperature excursions at a temperature of 5.9 Celsius degrees (C) for 10 hours and 8.8C for 8 hours (Product storage error). There were no previous temperature excursions and no other adverse events reported. This is one of three reports received from the same source.; Sender's Comments: US-009507513-2209USA003954: US-009507513-2209USA004041:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 20.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
no other adverse event occurred; Customer reported an AE for VARIVAX and MMRII. The caller said these products were administered to the patient after two temperature excursions occurred. Confirmed with caller no other AE occurred. Caller did not specify if she could be contacted. AE; This spontaneous report was received from a consumer concerning a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 02-SEP-2022, the patient was vaccinated with 1 dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (rHA) (M-M-R II) subcutaneous injection, lot #U019291, expiration date: 18-JUN-2023, (strength, and route of administration were not provided); and 1 dose of varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection, lot #U028164, expiration date: 09-SEP-2023, (strength, and route of administration were not provided), both administered as prophylaxis. The reporter stated that the vaccines were administered to the patient after two temperature excursions at a temperature of 5.9 Celsius degrees (C) for 10 hours, and 8.8C for 8 hours (product storage error). There were no previous temperature excursions and no other adverse events reported. This is one of several reports received from the same source.; Sender's Comments: US-009507513-2209USA004041:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Electrocardiogram normal
Hyperhidrosis
Hypophagia
Laboratory test
Lethargy
Pallor
Pulse abnormal
Symptomtext
Patient was given Varivax subcutaneous in left arm tricep area, MMR II right arm tricep area, and Hepatitis B Hepislav-B IM in left deltoid around 11:45 AM in a clinic setting by me. After giving all vaccines patient became lethargic, diaphoretic, pallor, and had a thready pulse of 20-30s after 1 minute. Patient legs were elevated and patient was reclined on exam table. EMS was called and patient remained lethargic, pale, with pulse in 20-30s, with pulse oximeter of 85% on room air (we do not have oxygen in this clinic). Gave patient an ammonia inhalant and patient began to be more conversant after 5 minutes. Pulse now in 40-50s. Paramedics arrived after 5 minutes, patient now alert and oriented, EKG performed and patient was in sinus rhythm. Patient was taken to Hospital for further work up but was discharged around 2:00 PM. Patient came back by clinic to thank clinic staff. Patient did inform staff after the situation that he had not eaten, had worked out and taken pre-workout before vaccination appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram normal
- Hospital-Tage
- -
- Labordaten
- 9/2 EKG-sinus rhythm
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE details were provided. No PQC.; Nurse calling in to report an AE for a patient that was administered a dose of MMR-II reconstituted with expired STERILE DILUENT. Per caller the patient was administered the dose of MMR-II today 19JUL2022 and the STERILE DILUENT expired 1JUL2022.; Nurse calling in to report an AE for a patient that was administered a dose of MMR-II reconstituted with expired STERILE DILUENT. Per caller the patient was administered the dose of MMR-II today 19JUL2022 and the STERILE DILUENT expired 1JUL2022.; This spontaneous report was received from a registered nurse concerning a patient of unknown gender and age. The patient's concomitant therapies, pertinent medical history, and drug reactions/allergies were not reported. On 19-JUL-2022, the patient was administered with a dose of 0.5 mL measles, mumps, and rubella (wistar RA 27-3) virus vaccine, live (recombinant human albumin (rHA)) (M-M-R II) (lot # U019291, expiration date 18-JUN-2023; strength was not reported), reconstituted with expired sterile diluent (STERILE DILUENT) (lot # S037027, expiration date 01-JUL-2022; strength was not reported) subcutaneously for prophylaxis (expired product administered, product preparation issue). No additional adverse event (AE) details were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
A 3rd dose of MMR was given by mistake. The patient had requested a menactra for school however the appointment was made for an MMR. Per vaccination site the patient did not have a 2nd dose of MMR so the dose was given. However, when the patient came back with a vaccination card a 2nd dose was given 4/3/2015 at another location. So the patient got 3 total doses of MMR. The patient is ok no side effects or concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
Patient scheduled for MMR but received Varicella vaccine instead. Error caught and MMR documented as administered on 5/25/22 as well. No adverse effects documented from administration of Varicella vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- HTN, OSA, GERD, hypothyroid, anxiety, prediabetes
- Andere Medikamente
- Buspar, chlorthalidone, citalopram, clonidine, ibuprofen, norgestimate-ethinyl estradiol, Omega 3, omeprazole, potassium chloride, NP Thyroid
- Allergien
- penicillin, Wellbutrin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Salivary hypersecretion
Strawberry tongue
Symptomtext
Strawberry tongue and excessive saliva
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Salivary hypersecretion
- Hospital-Tage
- -
- Labordaten
- Physical exam
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- none
- Andere Medikamente
- Clartian and montelukast
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Symptomtext
ADMINISTRATION ERROR: A Moderna Booster 0.25 mL was given by the Intradermal route instead of by the Intramuscular route when both a TB skin test and the Moderna booster were to be administered at the same visit. Vaccines were administered by RN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Symptomtext
no adverse reaction. Gave patient dose IM instead of SQ. Manufacturer said it was okay and not to repeat dose. Patient is aware
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -